Katalóg evidencie publikačnej činnosti PU


ID záznamu:PU.Prešov.2012070309080920
Kategória:ADC
Autor:Dojčáková Dana (40%)
Autor:Bernasovská Jarmila (10%)
Autor:Mačeková Soňa (10%)
Autor:Bôžiková Alexandra (10%)
Autor:Bernasovský Ivan (5%)
Autor:Bališinová Alena (3%)
Autor:Sovičová Adriana (5%)
Autor:Behulová Regína (3%)
Autor:Petrejčíková Eva (5%)
Autor:Soták Miroslav (4%)
Autor:Boroňová Iveta (5%)
Názov:Unique frequencies of HFE gene variants in Roma/Gypsies [print, elektronický dokument]
Zdroj:Journal of Applied Genetics [print]
Lokácia:Roč. 53, č. 2. - Berlín : Springer International Publishing AG, (2012), s. 183-187
ISSN:1234-1983. - ISSN 2190-3883
Ohlas:[1] 2014. ERICKSON, R.P., MITCHISON, N.A. The low frequency of recessive disease: insights from ENU mutagenesis, severity of disease phenotype, GWAS associations, and demography: an analytical review. In Journal of applied genetics, ISSN 1234-1983. 2014, vol. 55, no. 3, s. 319-327.
Ohlas:[1] 2015. MASINDOVA, I., SOLTYSOVA, A., VARGA, L. et al. MARVELD2 (DFNB49) Mutations in the hearing impaired Central European Roma population - prevalence, clinical impact and the common origin. In PLoS one, ISSN 1932-6203. 2015, vol. 10, no. 4.
Ohlas:[1] 2015. MCCULLOUGH, J.M., HEATH, K.M., SMITH, A.M. Hemochromatosis: Niche construction and the genetic domino eff ect in the European Neolithic. In Human biology, ISSN 0018-7143. 2015, vol. 87, no. 1, s. 39-58.
Ohlas:[1] 2015. BARTON, J.C., EDWARDS, C.Q., ACTON, R.T. HFE gene: Structure, function, mutations, and associated iron abnormalities. In Gene, ISSN 0378-1119. 2015, vol. 574, no. 2, s. 179-192.
Ohlas:[1] 2016. HEATH, K.M., AXTON, J.H., MCCULLOUGH, J.M. et al. The evolutionary adaptation of the C282Y mutation to culture and climate during the European Neolithic. In American journal of physical anthropology, ISSN 0002-9483. 2016, vol. 160, no. 1, s. 86-101.
Ohlas:[1] 2013. ROSTAS, A.R., NAGY-IULIUS, B. A note on roma mental health and the statement by Geza Jeszenszky. In Corvinus journal of sociology and social policy, ISSN 2061-5558. 2013, vol. 4, no. 2, s. 89-97.
Ohlas:[1] 2023. JATTA, F., HAJAR, CH.G.N., ZULKAFLI, Z. et al. The genetic landscape of hereditary haemochromatosis. In Genetic disorders and rare diseases : current updates. New York : NOVA Science Publishers, 2023, s. 251-270. ISBN 979-889113031-9. SCOPUS.